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rs878853355

From SNPedia

Orientationplus
Geno Mag Summary
(CTC;CTC) 0 common in clinvar
Make rs878853355(CTC;TT)
Make rs878853355(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position111968225
GeneMERTK
is asnp
is mentioned by
dbSNPrs878853355
ebirs878853355
HLIrs878853355
Exacrs878853355
Varsomers878853355
Maprs878853355
PheGenIrs878853355
hapmaprs878853355
1000 genomesrs878853355
hgdprs878853355
ensemblrs878853355
gopubmedrs878853355
geneviewrs878853355
scholarrs878853355
googlers878853355
pharmgkbrs878853355
gwascentralrs878853355
openSNPrs878853355
23andMers878853355
23andMe allrs878853355
SNP Nexus

SNPshotrs878853355
SNPdbers878853355
MSV3drs878853355
GWAS Ctlgrs878853355
Max Magnitude0
ClinVar
Risk rs878853355(TT;TT)
Alt rs878853355(TT;TT)
Reference rs878853355(CTC;CTC)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene MERTK
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000002.11:g.112725802_112725804delCTCinsTT
CLNSRC
CLNACC RCV000225588.1,